Sulfamethoxazole and Trimethoprim
- Product NDC
- 60687-531
- 11-digit product format
- 606870531
- Labeler code
- 60687
- Product ID
- 60687-531_d9543b2f-6b2f-5c86-e053-2a95a90a3a37
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sulfamethoxazole and Trimethoprim
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA076899
- Marketing category
- ANDA
- Marketing start
- 2020-02-11
- Marketing end
- 2023-09-30
- Substance
- SULFAMETHOXAZOLE; TRIMETHOPRIM
- Active strength
- 800 mg/1; mg/1
- Pharmacologic classes
- Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Dihydrofolate Reductase Inhibitor Antibacterial [EPC], Dihydrofolate Reductase Inhibitors [MoA], Organic Cation Transporter 2 Inhibitors [MoA], Sulfonamide Antimicrobial [EPC], Sulfonamides [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-531-01 | 60687053101 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-531-01) > 1 TABLET in 1 BLISTER PACK (60687-531-11) | 100 blister pack | 2019-12-16 | 0000-00-00 | No | No | Current |